Mouse neural tube organoids self-organize floorplate through BMP-mediated cluster competition

Dev Cell. 2024 Aug 5;59(15):1940-1953.e10. doi: 10.1016/j.devcel.2024.04.021. Epub 2024 May 21.

Abstract

During neural tube (NT) development, the notochord induces an organizer, the floorplate, which secretes Sonic Hedgehog (SHH) to pattern neural progenitors. Conversely, NT organoids (NTOs) from embryonic stem cells (ESCs) spontaneously form floorplates without the notochord, demonstrating that stem cells can self-organize without embryonic inducers. Here, we investigated floorplate self-organization in clonal mouse NTOs. Expression of the floorplate marker FOXA2 was initially spatially scattered before resolving into multiple clusters, which underwent competition and sorting, resulting in a stable "winning" floorplate. We identified that BMP signaling governed long-range cluster competition. FOXA2+ clusters expressed BMP4, suppressing FOXA2 in receiving cells while simultaneously expressing the BMP-inhibitor NOGGIN, promoting cluster persistence. Noggin mutation perturbed floorplate formation in NTOs and in the NT in vivo at mid/hindbrain regions, demonstrating how the floorplate can form autonomously without the notochord. Identifying the pathways governing organizer self-organization is critical for harnessing the developmental plasticity of stem cells in tissue engineering.

Keywords: developmental biology; floorplate; neural tube; organoids; pattern formation; self-organization; stem cell differentiation; stem cells.

MeSH terms

  • Animals
  • Bone Morphogenetic Protein 4* / metabolism
  • Bone Morphogenetic Proteins / metabolism
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Gene Expression Regulation, Developmental
  • Hedgehog Proteins / genetics
  • Hedgehog Proteins / metabolism
  • Hepatocyte Nuclear Factor 3-beta / genetics
  • Hepatocyte Nuclear Factor 3-beta / metabolism
  • Mice
  • Neural Tube* / cytology
  • Neural Tube* / metabolism
  • Notochord* / cytology
  • Notochord* / metabolism
  • Organoids* / cytology
  • Organoids* / metabolism
  • Signal Transduction

Substances

  • noggin protein
  • Bone Morphogenetic Protein 4
  • Hepatocyte Nuclear Factor 3-beta
  • Hedgehog Proteins
  • Foxa2 protein, mouse
  • Carrier Proteins
  • Bmp4 protein, mouse
  • Shh protein, mouse
  • Bone Morphogenetic Proteins